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For other serious unexpected adverse drug reactions, Korean regulations typically require notification within 7 days, with a full report within 15 days analogous to EUs SUSAR reporting timelines, but sponsors cannot assume that reporting to EudraVigilance or the EMA alone suffices

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Servono trial specificamente disegnati per la MASH per valutare leffettivo impatto epatico di retatrutide, tema ripreso nellarticolo Retatrutide e CagriSema: i nuovi farmaci anti-obesit che cambieranno la terapia